research use only

VBIT-12 VDAC inhibitor

Cat.No.S8936

VBIT-12 is a potent inhibitor of Voltage-dependent anion-selective channel 1 (VDAC1), directly interacting with purified VDAC1, reducing its channel conductance and preventing VDAC1 oligomerization.
VBIT-12 VDAC inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 417.50

Quality Control

Batch: S893601 DMSO]83 mg/mL]false]Water]2 mg/mL]false]Ethanol]Insoluble]false Purity: 98.69%
98.69

Chemical Information, Storage & Stability

Molecular Weight 417.50 Formula

C25H27N3O3

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 2089227-65-4 -- Storage of Stock Solutions

Synonyms N/A Smiles C1CN(CCC1(C(=O)NCC(=O)O)NC2=CC=CC=C2)CC3=CC=CC4=CC=CC=C43

Solubility

In vitro
Batch:

DMSO : 83 mg/mL (198.8 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 2 mg/mL

Ethanol : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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%DMSO %

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

Targets/IC50/Ki
VDAC1 [1]
In vitro

VBIT-12 directly interacts with purified VDAC1 and reduces its channel conductance. This compound interferes with VDAC1 oligomerization and thus with the pro-apoptotic action of VDAC1 when the levels of expression are abnormal, but have no effect on cells under physiological conditions.[2]

In vivo

The effect of VBIT-12 on induction of startle habituation and prepulse inhibition (PPI) in animals is examined via novelty suppressed feeding test, sweet preference model of anhedonia and forced swim test (FST) model for despair. This compound interacts with the Voltage-Dependent Anion Channel (VDAC) and can be used for the treatment of central nervous system (CNS) disorders and diseases.[1]

References

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